128 research outputs found
Study of transition temperatures in superconductors Final report, 11 Mar. 1968 - 10 Mar. 1970
Thermodynamic and electrical properties of niobium stannide and other superconductor
Study of transition temperatures in superconductors Quarterly progress report, 11 Jun. - 10 Sep. 1968
Superconducting properties of niobium-tin alloy and large single crystal growt
KELVIN: A Software Package for Rigorous Measurement of Statistical Evidence in Human Genetics
This paper describes the software package KELVIN, which supports the PPL (posterior probability of linkage) framework for the measurement of statistical evidence in human (or more generally, diploid) genetic studies. In terms of scope, KELVIN supports two-point (trait-marker or marker-marker) and multipoint linkage analysis, based on either sex-averaged or sex-specific genetic maps, with an option to allow for imprinting; trait-marker linkage disequilibrium (LD), or association analysis, in case-control data, trio data, and/or multiplex family data, with options for joint linkage and trait-marker LD or conditional LD given linkage; dichotomous trait, quantitative trait and quantitative trait threshold models; and certain types of gene-gene interactions and covariate effects. Features and data (pedigree) structures can be freely mixed and matched within analyses. The statistical framework is specifically tailored to accumulate evidence in a mathematically rigorous way across multiple data sets or data subsets while allowing for multiple sources of heterogeneity, and KELVIN itself utilizes sophisticated software engineering to provide a powerful and robust platform for studying the genetics of complex disorders
Superconductivity in Dense Wires
becomes superconducting just below 40 K. Whereas porous
polycrystalline samples of can be synthesized from boron powders, in
this letter we demonstrate that dense wires of can be prepared by
exposing boron filaments to vapor. The resulting wires have a diameter of
160 , are better than 80% dense and manifest the full shielding in the superconducting state. Temperature-dependent
resistivity measurements indicate that is a highly conducting metal in
the normal state with = 0.38 -. Using this value, an
electronic mean free path, can be estimated, indicating
that wires are well within the clean limit. , , and
data indicate that manifests comparable or better superconducting
properties in dense wire form than it manifests as a sintered pellet.Comment: Figures' layout fixe
A Review of the Properties of Nb3Sn and Their Variation with A15 Composition, Morphology and Strain State
This article gives an overview of the available literature on simplified,
well defined (quasi-)homogeneous laboratory samples. After more than 50 years
of research on superconductivity in Nb3Sn, a significant amount of results are
available, but these are scattered over a multitude of publications. Two
reviews exist on the basic properties of A15 materials in general, but no
specific review for Nb3Sn is available. This article is intended to provide
such an overview. It starts with a basic description of the Niobium-Tin
intermetallic. After this it maps the influence of Sn content on the the
electron-phonon interaction strength and on the field-temperature phase
boundary. The literature on the influence of Cu, Ti and Ta additions will then
be briefly summarized. This is followed by a review on the effects of grain
size and strain. The article is concluded with a summary of the main results.Comment: Invited Topical Review for Superconductor, Science and Technology.
Provisionally scheduled for July 200
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PEDSnet: a National Pediatric Learning Health System
A learning health system (LHS) integrates research done in routine care settings, structured data capture during every encounter, and quality improvement processes to rapidly implement advances in new knowledge, all with active and meaningful patient participation. While disease-specific pediatric LHSs have shown tremendous impact on improved clinical outcomes, a national digital architecture to rapidly implement LHSs across multiple pediatric conditions does not exist. PEDSnet is a clinical data research network that provides the infrastructure to support a national pediatric LHS. A consortium consisting of PEDSnet, which includes eight academic medical centers, two existing disease-specific pediatric networks, and two national data partners form the initial partners in the National Pediatric Learning Health System (NPLHS). PEDSnet is implementing a flexible dual data architecture that incorporates two widely used data models and national terminology standards to support multi-institutional data integration, cohort discovery, and advanced analytics that enable rapid learning
Complex-Orbital Order in Fe_3O_4 and Mechanism of the Verwey Transition
Electronic state and the Verwey transition in magnetite (Fe_3O_4) are studied
using a spinless three-band Hubbard model for 3d electrons on the B sites with
the Hartree-Fock approximation and the exact diagonalisation method.
Complex-orbital, e.g., 1/sqrt(2)[|zx> + i |yz>], ordered (COO) states having
noncollinear orbital moments ~ 0.4 mu_B on the B sites are obtained with the
cubic lattice structure of the high-temperature phase. The COO state is a novel
form of magnetic ordering within the orbital degree of freedom. It arises from
the formation of Hund's second rule states of spinless pseudo-d molecular
orbitals in the Fe_4 tetrahedral units of the B sites and ferromagnetic
alignment of their fictitious orbital moments. A COO state with longer
periodicity is obtained with pseudo-orthorhombic Pmca and Pmc2_1 structures for
the low-temperature phase. The state spontaneously lowers the crystal symmetry
to the monoclinic and explains experimentally observed rhombohedral cell
deformation and Jahn-Teller like distortion. From these findings, we consider
that at the Verwey transition temperature, the COO state remaining to be
short-range order impeded by dynamical lattice distortion in high temperature
is developed into that with long-range order coupled with the monoclinic
lattice distortion.Comment: 16 pages, 13 figures, 6 tables, accepted for publication in J. Phys.
Soc. Jp
A genome-wide scan for common alleles affecting risk for autism
Although autism spectrum disorders (ASDs) have a substantial genetic basis, most of the known genetic risk has been traced to rare variants, principally copy number variants (CNVs). To identify common risk variation, the Autism Genome Project (AGP) Consortium genotyped 1558 rigorously defined ASD families for 1 million single-nucleotide polymorphisms (SNPs) and analyzed these SNP genotypes for association with ASD. In one of four primary association analyses, the association signal for marker rs4141463, located within MACROD2, crossed the genome-wide association significance threshold of P < 5 × 10−8. When a smaller replication sample was analyzed, the risk allele at rs4141463 was again over-transmitted; yet, consistent with the winner's curse, its effect size in the replication sample was much smaller; and, for the combined samples, the association signal barely fell below the P < 5 × 10−8 threshold. Exploratory analyses of phenotypic subtypes yielded no significant associations after correction for multiple testing. They did, however, yield strong signals within several genes, KIAA0564, PLD5, POU6F2, ST8SIA2 and TAF1C
Behavioral and molecular genetics of reading-related AM and FM detection thresholds
Auditory detection thresholds for certain frequencies of both amplitude modulated (AM) and frequency modulated (FM) dynamic auditory stimuli are associated with reading in typically developing and dyslexic readers. We present the first behavioral and molecular genetic characterization of these two auditory traits. Two extant extended family datasets were given reading tasks and psychoacoustic tasks to determine FM 2 Hz and AM 20 Hz sensitivity thresholds. Univariate heritabilities were significant for both AM (h2 = 0.20) and FM (h2 = 0.29). Bayesian posterior probability of linkage (PPL) analysis found loci for AM (12q, PPL = 81 %) and FM (10p, PPL = 32 %; 20q, PPL = 65 %). Bivariate heritability analyses revealed that FM is genetically correlated with reading, while AM was not. Bivariate PPL analysis indicates that FM loci (10p, 20q) are not also associated with reading
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Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.
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